A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3328575



Internal ID15175562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155217426..155219124hg38UCSC Ensembl
Innerchr6:155218124..155218426hg38UCSC Ensembl
Outerchr6:155216426..155220124hg38UCSC Ensembl
chr6:155538560..155540258hg19UCSC Ensembl
Innerchr6:155539258..155539560hg19UCSC Ensembl
Outerchr6:155537560..155541258hg19UCSC Ensembl
chr6:155580252..155581950hg18UCSC Ensembl
Innerchr6:155581252..155580950hg18UCSC Ensembl
Outerchr6:155579252..155582950hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695064
SamplesNA19239
Known GenesTIAM2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3328575
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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